Canonical Allele Identifier: PA2826973896
Gene: SMARCB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790550
ClinVar RCV Id: RCV002428550 RCV003720628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304875.1:p.Gly71Arg
CA10145878
NM_001317946.2:c.211G>A
CA410933606
NM_001317946.2:c.211G>C